Canonical Allele Identifier: CA618424550
Gene: FAM81A HGNC NCBI

Linked Data

dbSNP Id: rs1207759973
gnomAD v2: 15-59711622-C-A
gnomAD v3: 15-59419423-C-A
gnomAD v4: 15-59419423-C-A
MyVariant Identifiers: chr15:g.59711622C>A (hg19) chr15:g.59419423C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.59419423C>A , CM000677.2:g.59419423C>A GRCh38
NC_000015.9:g.59711622C>A , CM000677.1:g.59711622C>A GRCh37
NC_000015.8:g.57498914C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000558348.5:c.-78+17065C>A ENSP00000453918.1:n.-78+17065C>A
ENST00000560394.5:c.-78+17065C>A ENSP00000452962.1:n.-78+17065C>A
XM_006720399.1:c.-78+17065C>A XP_006720462.1:n.-78+17065C>A
XM_011521248.1:c.-22+17065C>A XP_011519550.1:n.-22+17065C>A
XM_011521248.2:c.-22+17065C>A XP_011519550.1:n.-22+17065C>A
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